Liaño Riera Miryam, Santiago Sáez Andrés, García Martín Ángel, Gómez Serrano Manuel, Minoretti Piercarlo
Legal Medicine, Psychiatry, and Pathology, Complutense University of Madrid, Madrid, ESP.
Legal Medicine, Hospital Clinico San Carlos, Madrid, ESP.
Cureus. 2024 Jan 4;16(1):e51650. doi: 10.7759/cureus.51650. eCollection 2024 Jan.
Background Insomnia and poor sleep are leading modifiable risk factors for cardiovascular disease. Given the high susceptibility of airline pilots (APs) to sleep disturbances, we sought to investigate the hypothesis that poor sleep in this professional group correlates with alterations in plasma biochemical markers that would reflect critical aspects in the pathophysiology of cardiometabolic disorders. Methods In this preliminary cross-sectional study, we examined the relation of poor sleep to fourteen plasma biomarkers reflecting multiple cardiometabolic pathways in a convenience sample of 117 male APs. The Pittsburgh Sleep Quality Index (PSQI) was used to categorize the participants into good sleepers (n = 70, 59.8%; PSQI scores from 0 to 4) and poor sleepers (n = 47, 40.2%; PSQI scores of 5 or higher). The concentrations of biomarkers were compared between the two groups using both univariable and multivariable analyses. Results Compared to good sleepers, APs identified as poor sleepers exhibited significantly different levels of four plasma cardiometabolic biochemical markers in univariable analysis. However, in multivariable-adjusted analysis, only three biomarkers, adiponectin, fibroblast growth factor (FGF)-21, and growth differentiation factor (GDF)-15, remained independently associated with poor sleep. Conclusion Poor sleep quality in APs correlates with lower plasma concentrations of adiponectin and elevated levels of FGF-21 and GDF-15. Further longitudinal studies are required to elucidate the role of these biomarkers in the link between sleep disturbances and cardiometabolic risk in this professional group.
失眠和睡眠不佳是心血管疾病的主要可改变风险因素。鉴于航空公司飞行员(APs)极易出现睡眠障碍,我们试图研究这样一个假设,即该职业群体的睡眠不佳与血浆生化标志物的改变相关,这些改变能够反映心脏代谢紊乱病理生理学的关键方面。方法:在这项初步的横断面研究中,我们在117名男性APs的便利样本中,研究了睡眠不佳与反映多种心脏代谢途径的14种血浆生物标志物之间的关系。使用匹兹堡睡眠质量指数(PSQI)将参与者分为睡眠良好者(n = 70,59.8%;PSQI评分0至4)和睡眠不佳者(n = 47,40.2%;PSQI评分5或更高)。使用单变量和多变量分析比较两组生物标志物的浓度。结果:在单变量分析中,与睡眠良好者相比,被确定为睡眠不佳的APs有四种血浆心脏代谢生化标志物的水平存在显著差异。然而,在多变量调整分析中,只有三种生物标志物,即脂联素、成纤维细胞生长因子(FGF)-21和生长分化因子(GDF)-15,仍然与睡眠不佳独立相关。结论:APs的睡眠质量不佳与血浆脂联素浓度降低以及FGF-21和GDF-15水平升高相关。需要进一步的纵向研究来阐明这些生物标志物在该职业群体睡眠障碍与心脏代谢风险之间联系中的作用。